Patrizia Sabatelli
Patrizia Sabatelli
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Cited by
Cited by
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
WA Irwin, N Bergamin, P Sabatelli, C Reggiani, A Megighian, L Merlini, ...
Nature genetics 35 (4), 367-371, 2003
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
P Grumati, L Coletto, P Sabatelli, M Cescon, A Angelin, E Bertaggia, ...
Nature medicine 16 (11), 1313-1320, 2010
POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome
J van Reeuwijk, M Janssen, C van den Elzen, DBV De Bernabé, ...
Journal of medical genetics 42 (12), 907-912, 2005
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
O Camacho Vanegas, E Bertini, RZ Zhang, S Petrini, C Minosse, ...
Proceedings of the National Academy of Sciences 98 (13), 7516-7521, 2001
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
L Merlini, A Angelin, T Tiepolo, P Braghetta, P Sabatelli, A Zamparelli, ...
Proceedings of the National Academy of Sciences 105 (13), 5225-5229, 2008
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
A Angelin, T Tiepolo, P Sabatelli, P Grumati, N Bergamin, C Golfieri, ...
Proceedings of the National Academy of Sciences 104 (3), 991-996, 2007
EMILIN-1 deficiency induces elastogenesis and vascular cell defects
M Zanetti, P Braghetta, P Sabatelli, I Mura, R Doliana, A Colombatti, ...
Molecular and cellular biology 24 (2), 638-650, 2004
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human
M Neri, S Torelli, S Brown, I Ugo, P Sabatelli, L Merlini, P Spitali, ...
Neuromuscular Disorders 17 (11-12), 913-918, 2007
Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy
E Demir, P Sabatelli, V Allamand, A Ferreiro, B Moghadaszadeh, ...
The American Journal of Human Genetics 70 (6), 1446-1458, 2002
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy
L Cartegni, MR Di Barletta, R Barresi, S Squarzoni, P Sabatelli, N Maraldi, ...
Human molecular genetics 6 (13), 2257-2264, 1997
Preclinical PK and PD studies on 2′-O-methyl-phosphorothioate RNA antisense oligonucleotides in the mdx mouse model
H Heemskerk, C De Winter, P Van Kuik, N Heuvelmans, P Sabatelli, ...
Molecular Therapy 18 (6), 1210-1217, 2010
The cyclophilin inhibitor Debio 025 normalizes mitochondrial function, muscle apoptosis and ultrastructural defects in Col6a1−/− myopathic mice
T Tiepolo, A Angelin, E Palma, P Sabatelli, L Merlini, L Nicolosi, F Finetti, ...
British journal of pharmacology 157 (6), 1045-1052, 2009
Emilin1 Deficiency Causes Structural and Functional Defects of Lymphatic Vasculature
C Danussi, P Spessotto, A Petrucco, B Wassermann, P Sabatelli, ...
Molecular and cellular biology 28 (12), 4026-4039, 2008
Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice
E Palma, T Tiepolo, A Angelin, P Sabatelli, NM Maraldi, E Basso, ...
Human molecular genetics 18 (11), 2024-2031, 2009
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy
I Filesi, F Gullotta, G Lattanzi, MR D'Apice, C Capanni, AM Nardone, ...
Physiological genomics 23 (2), 150-158, 2005
Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts
P Sabatelli, P Bonaldo, G Lattanzi, P Braghetta, N Bergamin, C Capanni, ...
Matrix Biology 20 (7), 475-486, 2001
Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: implications for congenital muscular dystrophy types Ullrich and Bethlem
Y Zou, RZ Zhang, P Sabatelli, ML Chu, CG Bönnemann
Journal of Neuropathology & Experimental Neurology 67 (2), 144-154, 2008
The 180-kDa isoform of topoisomerase II is localized in the nucleolus and belongs to the structural elements of the nucleolar remnant
N Zini, AM Martelli, P Sabatelli, S Santi, C Negri, GCBA Ricotti, ...
Experimental cell research 200 (2), 460-466, 1992
Nuclear changes in a case of X‐linked Emery‐Dreifuss muscular dystrophy
A Ognibene, P Sabatelli, S Petrini, S Squarzoni, M Riccio, S Santi, ...
Muscle & Nerve: Official Journal of the American Association of …, 1999
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop, 23–24 November 2001, Naarden, The Netherlands
G Pepe, E Bertini, P Bonaldo, K Bushby, B Giusti, M De Visser, ...
Neuromuscular Disorders 12 (10), 984-993, 2002
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